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Psychotropic drug influences on brain acetylcholine utilization

dc.contributor.authorDomino, Edward F.en_US
dc.contributor.authorWilson, Ann E.en_US
dc.date.accessioned2006-09-11T17:42:58Z
dc.date.available2006-09-11T17:42:58Z
dc.date.issued1972-12en_US
dc.identifier.citationDomino, Edward F.; Wilson, Ann E.; (1972). "Psychotropic drug influences on brain acetylcholine utilization." Psychopharmacologia 25(4): 291-298. <http://hdl.handle.net/2027.42/46382>en_US
dc.identifier.issn0033-3158en_US
dc.identifier.issn1432-2072en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46382
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=5051143&dopt=citationen_US
dc.description.abstractThe cholinergic antisynthesis agent HC-3 was given intraventricularly to young male rats 20–30 days old to deplete brain acetylcholine (ACh). The rate of HC-3 induced depletion of ACh was used as an index of ACh utilization. Total brain ACh was determined following various doses of chlordiazepoxide, pentobarbital, chlorpromazine, methotrimeprazine, imipramine, morphine, d -amphetamine, scopolamine, LSD-25, and phencyclidine given i.p. alone and after intraventricular administration of HC-3. It was found that psychotropic drugs have marked differential effects on the rate of HC-3 induced ACh depletion.en_US
dc.format.extent416991 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherLSD-25en_US
dc.subject.otherMorphineen_US
dc.subject.otherPsychiatryen_US
dc.subject.otherD -Amphetamineen_US
dc.subject.otherPsychotropic Drugsen_US
dc.subject.otherChlorpromazineen_US
dc.subject.otherPheneyclidineen_US
dc.subject.otherAcetylcholineen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherChlordiazepoxideen_US
dc.subject.otherImipramineen_US
dc.subject.otherMethotrimeprazineen_US
dc.subject.otherScopolamineen_US
dc.titlePsychotropic drug influences on brain acetylcholine utilizationen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMichigan Neuropsychopharmacology Research Program, Department of Pharmacology, University of Michigan, Ann Arbor; Lafayette Clinic, Detroit, USAen_US
dc.contributor.affiliationumMichigan Neuropsychopharmacology Research Program, Department of Pharmacology, University of Michigan, Ann Arbor; Lafayette Clinic, Detroit, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid5051143en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46382/1/213_2004_Article_BF00421968.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00421968en_US
dc.identifier.sourcePsychopharmacologiaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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